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Rare combination of simple virilizing form of 21-hydroxylase deficiency, Graves’ disease and 47, XXX in a woman: A case report

Coexistence of congenital adrenal hyperplasia due to 21-hydroxylase deficiency, Graves’ disease and 47, XXX is rare. We report a case of a 25-year-old woman presented with masculine appearance, hirsutism and enlarged clitoris. Lab tests showed elevated serum 17 hydroxyprogesterone, testosterone, deh...

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Detalles Bibliográficos
Autores principales:	Liang, Dong, Han, Minmin, Xu, Linxin, Ren, Yi, Zhang, Yi, Yin, Jianhong, Yang, Jing, Liu, Yunfeng
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2022
Materias:	4300
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622681/ https://www.ncbi.nlm.nih.gov/pubmed/36316845 http://dx.doi.org/10.1097/MD.0000000000031443

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